The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
125362331 12536233 1 I 20160622 20160630 20160707 20160707 EXP CA-AMGEN-CANSL2016085866 AMGEN 46.00 YR A F Y 100.00000 KG 20160707 OT CA CA

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
125362331 12536233 1 PS ARANESP DARBEPOETIN ALFA 1 Subcutaneous 20 MUG, QWK 103951 20 UG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125362331 12536233 1 Nephrogenic anaemia

Outcome of event

Event ID CASEID OUTC COD
125362331 12536233 OT
125362331 12536233 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125362331 12536233 Asthenia
125362331 12536233 Back pain
125362331 12536233 Decubitus ulcer
125362331 12536233 Dizziness
125362331 12536233 Fatigue
125362331 12536233 Haemoglobin abnormal
125362331 12536233 Malaise
125362331 12536233 Urinary tract infection

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125362331 12536233 1 20160622 0